C3 glomerulopathy: Difference between revisions

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{{C3 glomerulopathy}}                                                                 
{{SI}}                                                                 
{{CMG}} {{APM}};{{AE}}{{Vbe}}
{{CMG}};{{AE}} {{Vbe}} {{ADG}}
 
'''''For more information of Complement mediated glomerular disorders, [[Complement mediated glomerular disorders|Click here]]'''''
   
   
{{SK}} glomerulonephritis; C3 glomerulonephritis; dense deposit disease
{{SK}} Glomerulonephritis; C3 glomerulonephritis; dense deposit disease


==[[C3 glomerulopathy overview|Overview]]==
==Overview==
C3 glomerulopathy is a disorder of [[complement]] system, and can be due to inherited or acquired [[complement]] dysregulation and activation of the "alternative pathway". The category of C3 [[glomerulopathy]] contains a diverse group of disorders, including those leading to the [[inflammatory]] forms of C3 [[glomerulopathy]], namely C3 [[glomerulonephritis]] (C3GN), as wells as those presenting as [[dense deposit disease]] (DDD).  Both, C3GN and dense deposit disease are marked by C3 deposition along the [[capillary]] loop, the [[basement membrane]], and the [[mesangium]]. It is a  requirement for the [[diagnosis]] of C3 [[glomerulopathy]], that the presence of C3 deposits comes without any concomitant [[immunoglobulin]] deposition.   
[[C3 (complement)|C3]] [[glomerulopathy]] is a [[complement]] system dysregulatory disorder resulting in abnormal activation of the alternative pathway. C3 [[glomerulopathy]] includes C3 [[glomerulonephritis]] (C3GN) and [[dense deposit disease]] (DDD).  Both, C3GN and dense deposit disease are characterized by marked by C3 deposition along the [[capillary]] loop, the [[basement membrane]], and the [[mesangium]]. Identification of C3 deposits without any concomitant [[immunoglobulin]] deposition is characteristic for diagnosing C3 glomerulopathy. The activation of the [[Alternative Livelihood|alternative]] pathway of the [[complement]] system can be either due to [[inherited]], or [[acquired]] defects of the [[complement]] system. Gene mutations are the most common inherited causes while autoimmune disorders are responsible for acquired glomerulopathy.   


The activation of the [[Alternative Livelihood|alternative]] pathway of the [[complement]] system can be either due to [[inherited]], or [[acquired]] defects of the [[complement]] system. The inherited forms of [[complement]] dysregulation are due to numerous identified (and potentially yet to be identified) [[mutations]] of [[genes]] involved in [[complement]] pathway (see causes). The acquired forms of [[complement]] dysregulation are mostly due to [[autoimmunity]] against [[complement]] regulatory [[proteins]].
==Historical Perspective==
 
*In 1915, William C. Gunn was first to report an association of low [[Circulating immune complexes|circulating]] [[complement]] levels in [[patients]] with acute [[infection]] and [[Nephritic syndrome|nephritic]] presentation.
==[[C3 glomerulopathy historical perspective|Historical Perspective]]==
*Based on the William's observations, role of [[complement]] system in [[inflammatory]] [[glomerulonephritis]] was well described.<ref name="pmid13568372">{{cite journal |vauthors=SELIGMANN M, HANAU C |title=[Immuno-electrophoretic study of the blood of disseminated lupus erythematosus patients] |language=French |journal=Rev Hematol |volume=13 |issue=2 |pages=239–48 |date=1958 |pmid=13568372 |doi= |url=}}</ref><ref name="pmid14201535">{{cite journal |vauthors=WEST CD, NORTHWAY JD, DAVIS NC |title=SERUM LEVELS OF BETA-1C GLOBULIN, A COMPLEMENT COMPONENT, IN THE NEPHRITIDES, LIPOID NEPHROSIS, AND OTHER CONDITIONS |journal=J. Clin. Invest. |volume=43 |issue= |pages=1507–17 |date=August 1964 |pmid=14201535 |pmc=441951 |doi=10.1172/JCI105027 |url=}}</ref>
*In 1915 William C. Gunn reported on the [[Findings on urinalysis|finding]] of low [[Circulating immune complexes|circulating]] [[complement]] levels in [[patients]] with acute [[infection]] and [[Nephritic syndrome|nephritic]] presentation  
* In 1962, Jean Berger and Pierre Galle, Nephro-pathologists, was the first to identify [[dense]] [[Intramembranous ossification|intramembranous]] deposits on transmission [[EMERAS|EM]] <ref name="pmid13867660">{{cite journal| author=BERGER J, GALLE P| title=[Unusual change of the basal membranes of the kidney]. | journal=J Urol Nephrol (Paris) | year= 1962 | volume= 68 | issue=  | pages= 116-22 | pmid=13867660 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=13867660  }} </ref>.
*Later on, additional reports on the involvement of [[complement]] system in other forms of [[inflammatory]] [[glomerulonephritis]] were presented, and their role further established.<ref name="pmid13568372">{{cite journal |vauthors=SELIGMANN M, HANAU C |title=[Immuno-electrophoretic study of the blood of disseminated lupus erythematosus patients] |language=French |journal=Rev Hematol |volume=13 |issue=2 |pages=239–48 |date=1958 |pmid=13568372 |doi= |url=}}</ref><ref name="pmid14201535">{{cite journal |vauthors=WEST CD, NORTHWAY JD, DAVIS NC |title=SERUM LEVELS OF BETA-1C GLOBULIN, A COMPLEMENT COMPONENT, IN THE NEPHRITIDES, LIPOID NEPHROSIS, AND OTHER CONDITIONS |journal=J. Clin. Invest. |volume=43 |issue= |pages=1507–17 |date=August 1964 |pmid=14201535 |pmc=441951 |doi=10.1172/JCI105027 |url=}}</ref>
*Mathew TH, Kinaid Smith P coined the term dense deposit disease (DDD).<ref name="pmid20606628">{{cite journal |vauthors=Fakhouri F, Frémeaux-Bacchi V, Noël LH, Cook HT, Pickering MC |title=C3 glomerulopathy: a new classification |journal=Nat Rev Nephrol |volume=6 |issue=8 |pages=494–9 |date=August 2010 |pmid=20606628 |doi=10.1038/nrneph.2010.85 |url=}}</ref>
* In the year 1962, two renowned Nephro-pathologists, Jean Berger and Pierre Galle identified a rare [[glomerular]] [[lesion]] characterized by [[dense]] [[Intramembranous ossification|intramembranous]] deposits on transmission [[EMERAS|EM]] <ref name="pmid13867660">{{cite journal| author=BERGER J, GALLE P| title=[Unusual change of the basal membranes of the kidney]. | journal=J Urol Nephrol (Paris) | year= 1962 | volume= 68 | issue=  | pages= 116-22 | pmid=13867660 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=13867660  }} </ref>.
*The term Dense Deposit Disease (DDD) was coined and described to be a [[disease]] entity associated with under belonging to the category of  [[Membranoproliferative GN|membrano]]-[[Proliferative bronchiolitis|proliferative]] type [[Glomerulonephritis|glomerulonephritides]] (MPGN)  (Mathew TH, Kincaid-Smith P).
*It took almost 50 years, until [[C3 glomerulopathy]] was identified as an independent [[disease]] entity, leading to potentially new [[diagnostic]], [[therapeutic]] and [[prognostic]] opportunities. <ref name="pmid20606628">{{cite journal |vauthors=Fakhouri F, Frémeaux-Bacchi V, Noël LH, Cook HT, Pickering MC |title=C3 glomerulopathy: a new classification |journal=Nat Rev Nephrol |volume=6 |issue=8 |pages=494–9 |date=August 2010 |pmid=20606628 |doi=10.1038/nrneph.2010.85 |url=}}</ref>


==Classification==
==Classification==
 
*Initially, [[C3 (complement)|C3]] [[glomerulopathy]] was categorized as a variant of [[MPGN]], namely MPGN type 2. <ref name="pmid15800116">{{cite journal |vauthors=Appel GB, Cook HT, Hageman G, Jennette JC, Kashgarian M, Kirschfink M, Lambris JD, Lanning L, Lutz HU, Meri S, Rose NR, Salant DJ, Sethi S, Smith RJ, Smoyer W, Tully HF, Tully SP, Walker P, Welsh M, Würzner R, Zipfel PF |title=Membranoproliferative glomerulonephritis type II (dense deposit disease): an update |journal=J. Am. Soc. Nephrol. |volume=16 |issue=5 |pages=1392–403 |date=May 2005 |pmid=15800116 |doi=10.1681/ASN.2005010078 |url=}}</ref><ref name="pmid17018561">{{cite journal| author=Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B et al.| title=Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. | journal=J Med Genet | year= 2007 | volume= 44 | issue= 3 | pages= 193-9 | pmid=17018561 | doi=10.1136/jmg.2006.045328 | pmc=2598029 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17018561  }} </ref>  
 
*However in 2007, Servais A. et al described C3GN as an separate entity.
*Until recently, [[C3 glomerulopathy]] (C3 glomerulonephritis and DDD) were categorized under as a variant of [[MPGN]], namely MPGN type 2. <ref name="pmid15800116">{{cite journal |vauthors=Appel GB, Cook HT, Hageman G, Jennette JC, Kashgarian M, Kirschfink M, Lambris JD, Lanning L, Lutz HU, Meri S, Rose NR, Salant DJ, Sethi S, Smith RJ, Smoyer W, Tully HF, Tully SP, Walker P, Welsh M, Würzner R, Zipfel PF |title=Membranoproliferative glomerulonephritis type II (dense deposit disease): an update |journal=J. Am. Soc. Nephrol. |volume=16 |issue=5 |pages=1392–403 |date=May 2005 |pmid=15800116 |doi=10.1681/ASN.2005010078 |url=}}</ref>  
*C3 Glomerulopathy may be classified into 2 main subtypes based on the appearance of complement deposition in the glomerular basement membrane on EM:
*In 2007, Servais A. et al described C3GN as an entity by itself. C3 [[glomerulonephritis]] was described as [[glomerular]] [[disease]] with deposits made up of only C3 without the presence of any [[immunoglobulins]], that may or may not have a [[Membranoproliferative GN|membranoproliferative]] pattern <ref name="pmid17018561">{{cite journal| author=Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B et al.| title=Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome. | journal=J Med Genet | year= 2007 | volume= 44 | issue= 3 | pages= 193-9 | pmid=17018561 | doi=10.1136/jmg.2006.045328 | pmc=2598029 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17018561  }} </ref>.
**'''Dense deposit disease (DDD)'''
*[[Dense deposit disease]] refers to one subcategory of C3 [[glomerulopathy]] which is characterized by GBM deposits of C3 with characteristic appearance on electron micro graphs. Isolated C3 deposit in the glomerulus is the defining characteristics of C3 glomerulopathy. When deposit is linear, ribbon like and concentrated on the [[glomerular basement membrane]], it is referred to as the Dense Deposit Disease (DDD). Currently, it is unknown whether the distinction between C3 glomerulonephritis and DDD has any [[therapeutic]] or [[prognostic]] relevance.  
***Dense deposition of compliment in linear pattern.
*C3 Glomerulopathy may be classified into 2 main subtypes/groups:
**'''[[C3 (complement)|C3]] [[Glomerulonephritis]] (C3GN)'''
:*Dense Deposit Disease (DDD)- more common in children, and is frequently associated with [[lipodystrophy]].
***Isolated deposition of C3.
:*C3 [[Glomerulonephritis]] (C3GN)
 
==Pathophysiology==
==Pathophysiology==
*[[C3 glomerulopathy MRI|C3 glomerulopathy]] results from the appropriate or inappropriate [[Activation-Induced (Cytidine) Deaminase|activation]] of the [[Alternative Livelihood|alternative]] [[Pathways Health and Research Centre|pathway]] of the [[complement]] system.
*Excessive activation of the [[Alternative Livelihood|alternative]] complement [[Pathways Health and Research Centre|pathway]] is the inciting event in the pathogenesis of C3 glomerulopathy.<ref name="pmid8695987">{{cite journal |vauthors=Schwertz R, de Jong R, Gretz N, Kirschfink M, Anders D, Schärer K |title=Outcome of idiopathic membranoproliferative glomerulonephritis in children. Arbeitsgemeinschaft Pädiatrische Nephrologie |journal=Acta Paediatr. |volume=85 |issue=3 |pages=308–12 |date=March 1996 |pmid=8695987 |doi= |url=}}</ref>
*Activation of alternative pathway results in  excessive deposition of complement along the glomerular basement membrane.
*Pattern of  compliment deposition is regulated by:<ref name="pmid254845263">{{cite journal |vauthors=Thomas S, Ranganathan D, Francis L, Madhan K, John GT |title=Current concepts in C3 glomerulopathy |journal=Indian J Nephrol |volume=24 |issue=6 |pages=339–48 |date=November 2014 |pmid=25484526 |pmc=4244712 |doi=10.4103/0971-4065.134089 |url=}}</ref>
**Leukocytic chemotaxis
**Cytolytic effects of C5b-9


*The appropriate [[Activation-Induced (Cytidine) Deaminase|activation]] of [[complement system]] is under general circumstances triggered by [[infection]]. The inappropriate [[Activation-Induced (Cytidine) Deaminase|activation]] can be due to [[inherited]] or acquired [[disorders]] of [[complement]] pathway. Either a gain of function of complement “activators”, or a loss of function of complement “inhibitors” can lead to an activation of complement alternative pathway.
==== Physiology ====
* Spontaneous cleavage of [[C3 (complement)|C3]] to C3b results in activation of [[C3 convertase|C3 convertase.]]<ref name="pmid24161035">{{cite journal |vauthors=Noris M, Remuzzi G |title=Overview of complement activation and regulation |journal=Semin. Nephrol. |volume=33 |issue=6 |pages=479–92 |date=November 2013 |pmid=24161035 |pmc=3820029 |doi=10.1016/j.semnephrol.2013.08.001 |url=}}</ref>
* [[C3 convertase]] along with factor B and [[properdin]] catalyses the cascade of producing [[C5-convertase|C5 convertase]].
* [[C5]] convertse cleaves 5 to C5a initiating C5b-9 ( MAC complex)
* Physiologically activation of [[C5-convertase|C5 convertase]] is directly related to [[C3 convertase]].
* Factors that can influence and control [[C3 convertase]] activity include
** Serum protein
** Factor H (inhibits the [[C3 convertase]])


*Possible [[physiological]] and [[pathological]] [[Activation-Induced (Cytidine) Deaminase|activation]] mechanisms of the [[complement]] pathways which can contribute or lead to [[complement]] mediated [[glomerulopathy]]:
==== Pathogenesis ====
 
* Any mechanism by which C3 activity is increased leads to activation of alternate pathway activation resulting in complement deposition.<ref name="pmid254845262">{{cite journal |vauthors=Thomas S, Ranganathan D, Francis L, Madhan K, John GT |title=Current concepts in C3 glomerulopathy |journal=Indian J Nephrol |volume=24 |issue=6 |pages=339–48 |date=November 2014 |pmid=25484526 |pmc=4244712 |doi=10.4103/0971-4065.134089 |url=}}</ref><ref name="pmid23026947">{{cite journal |vauthors=Bomback AS, Appel GB |title=Pathogenesis of the C3 glomerulopathies and reclassification of MPGN |journal=Nat Rev Nephrol |volume=8 |issue=11 |pages=634–42 |date=November 2012 |pmid=23026947 |doi=10.1038/nrneph.2012.213 |url=}}</ref>
{| class="wikitable"
** C3 convertase autoantibody C3 nephritic factor
! colspan="2" |Activation of Classic Complement Pathway
** Loss of factor H
!Activation of the Mannose-Binding-Lectin Pathway
! colspan="4" |Activation of Alternative Complement Pathway
|-
| colspan="2" |Acquired
|Acquired
| colspan="3" |Acquired
|Inherited
|-
|Infection
|Apoptosis and necrosis
|Infection
|Infection
|Autoimmune disorder
|Paraneoplastic
|Genetic mutations
|}


==Causes==
==Causes==
Several [[genetic]] or acquired [[causes]] have been described to date:
Common causes of C3 glomerulopathy include:<ref name="pmid23728171">{{cite journal |vauthors=Holers VM |title=Human C3 glomerulopathy provides unique insights into complement factor H-related protein function |journal=J. Clin. Invest. |volume=123 |issue=6 |pages=2357–60 |date=June 2013 |pmid=23728171 |pmc=3668810 |doi=10.1172/JCI69684 |url=}}</ref>
* C3 [[mutations]]
* C3 [[mutations]]
* [[Complement]] Factor H (CFH):
* [[Mutation]] of Factor H (CHF)<ref name="pmid15163532">{{cite journal |vauthors=Rodríguez de Córdoba S, Esparza-Gordillo J, Goicoechea de Jorge E, Lopez-Trascasa M, Sánchez-Corral P |title=The human complement factor H: functional roles, genetic variations and disease associations |journal=Mol. Immunol. |volume=41 |issue=4 |pages=355–67 |date=June 2004 |pmid=15163532 |doi=10.1016/j.molimm.2004.02.005 |url=}}</ref>
Like the majority of [[complement]] factors, CFH is a small glycoprotein which is produced in the [[liver]], and circulates freely in the [[blood plasma]] . Several [[mutations]] in the CFH gene have been identified. While in type 1 [[mutations]] in this [[gene]] lead to a decrease in the level of functional CFH, the majority of mutations (type 2) do not affect the level of CFH, but rather decrease or diminish the function activity of this [[glycoprotein]]. [[Autoantibodies]] against CFH have been identified . <ref name="pmid29948306">{{cite journal |vauthors=Noris M, Donadelli R, Remuzzi G |title=Autoimmune abnormalities of the alternative complement pathway in membranoproliferative glomerulonephritis and C3 glomerulopathy |journal=Pediatr. Nephrol. |volume= |issue= |pages= |date=June 2018 |pmid=29948306 |doi=10.1007/s00467-018-3989-0 |url=}}</ref>
** CFH is a small glycoprotein which is produced in the [[liver]], and circulates freely in the [[blood plasma]] .  
 
** Primary role of factor H is to inhibit C3 convertase and thus not activating alternative complement pathway.
* [[Complement]] Factor I (CFI):
** Two types of mutations are of important significance
 
*** Type 1 [[mutations]] are associated with decreased levels of CFH.
* Membrane Cofactor [[Protein]] (MCP):
*** Type 2 mutations decrease or diminish the functional activity of CHF.
MCP is a [[transmembrane protein]], expressed by all [[Nucleated|nucleate]]<nowiki/>d [[cells]] and located at the [[cell]] surfaces. Together with [[Complement]] Factor I (CFI), MCP is required for the inactivation of C3b, which otherwise may initiate the formation of [[membrane attack complex]]. [[Mutations]] in the MCP gene can, similar to [[mutations]] in CFH lead to both, either a decrease in synthesis and expression of this [[protein]], or a decreased activity.
** [[Autoantibodies]] against CFH. <ref name="pmid29948306">{{cite journal |vauthors=Noris M, Donadelli R, Remuzzi G |title=Autoimmune abnormalities of the alternative complement pathway in membranoproliferative glomerulonephritis and C3 glomerulopathy |journal=Pediatr. Nephrol. |volume= |issue= |pages= |date=June 2018 |pmid=29948306 |doi=10.1007/s00467-018-3989-0 |url=}}</ref>


* C3 [[Nephritic syndrome|nephritic]] factor (C3bBb antibody)
* Mutation of membrane cofactor protein ( MCP)  
* Factor H [[antibody]]
** MCP is a<nowiki/> [[transmembrane protein]], expressed by all [[Nucleated|nucleate]]<nowiki/>d [[cells]] and located at the [[cell]] surfaces.
* Factor I [[antibody]]
** Together with [[Complement]] Factor I (CFI), MCP is required <nowiki/>for the inactivation of C3b,
* Factor H [[mutations]]
* Factor I [[mutations]]
* Factor B [[mutations]]
* CR1 mutations
* CFHRs [[mutations]]<ref name="pmid28729035">{{cite journal |vauthors=Togarsimalemath SK, Sethi SK, Duggal R, Le Quintrec M, Jha P, Daniel R, Gonnet F, Bansal S, Roumenina LT, Fremeaux-Bacchi V, Kher V, Dragon-Durey MA |title=A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathy |journal=Kidney Int. |volume=92 |issue=4 |pages=876–887 |date=October 2017 |pmid=28729035 |doi=10.1016/j.kint.2017.04.025 |url=}}</ref>


* Dense Deposit [[Disease]]
* Auto antibody against C3 called as [[Nephritic syndrome|nephritic]] factor (C3bBb antibody).<ref name="pmid28729035">{{cite journal |vauthors=Togarsimalemath SK, Sethi SK, Duggal R, Le Quintrec M, Jha P, Daniel R, Gonnet F, Bansal S, Roumenina LT, Fremeaux-Bacchi V, Kher V, Dragon-Durey MA |title=A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathy |journal=Kidney Int. |volume=92 |issue=4 |pages=876–887 |date=October 2017 |pmid=28729035 |doi=10.1016/j.kint.2017.04.025 |url=}}</ref>


==Differentiating C3 Glomerulopathy from other Diseases==
==Differentiating C3 Glomerulopathy from other Diseases==
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! style="background: #4479BA; width: 200px;" | {{fontcolor|#FFF|Mediacl condition}}
! style="background: #4479BA; width: 200px;" | {{fontcolor|#FFF|Medical condition}}
! style="background: #4479BA; width: 300px;" | {{fontcolor|#FFF| Differentiating features }}
! style="background: #4479BA; width: 300px;" | {{fontcolor|#FFF| Differentiating features }}
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==Epidemiology and Demographics==
==Epidemiology and Demographics==
* The [[prevalence]] of C3 [[glomerulopathy]] is approximately 3 per 100,000 individuals worldwide.
* The [[prevalence]] of [[C3 glomerulopathy MRI|C3 glomerulopathy]] is approximately 3 per 100,000 individuals worldwide.<ref name="pmid17675665">{{cite journal| author=Smith RJ, Alexander J, Barlow PN, Botto M, Cassavant TL, Cook HT et al.| title=New approaches to the treatment of dense deposit disease. | journal=J Am Soc Nephrol | year= 2007 | volume= 18 | issue= 9 | pages= 2447-56 | pmid=17675665 | doi=10.1681/ASN.2007030356 | pmc=4853920 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17675665  }} </ref>


===Age===
*[[Patients]] of all [[age]] groups may develop [[C3 glomerulopathy MRI|C3 glomerulopathy]] but it commonly affects young adults and children (Dense deposit disease)
*[[Patients]] of all [[age]] groups may develop C3 [[glomerulopathy]] but it commonly affects young adults and children (Dense deposit disease)


===Gender===
* C3 [[glomerulopathy]] affects [[men]] and [[Women's College Hospital|women]] equally.
* C3 [[glomerulopathy]] affects [[men]] and [[Women's College Hospital|women]] equally.


===Race===
*There is no racial predilection for [[C3 glomerulopathy MRI|C3 glomerulopathy]].
*There is no racial predilection for [[C3 glomerulopathy MRI|C3 glomerulopathy]].


==Risk Factors==
==Risk Factors==
* [[Risk-benefit analysis|Risk]] [[Factors 2a|factors]] in the development of [[C3 glomerulopathy]]:
Common risk factors in the development of [[C3 glomerulopathy MRI|C3 glomerulopathy]] include:
* [[Family]] [[History and Physical examination|history]] of C3 glomerulopathy
* H/O  [[autoimmune disorders]]


* [[Family]] [[History and Physical examination|history]]
==Screening==
* Having family members with [[autoimmune disorders]]
*There is insufficient evidence to recommend routine screening for C3 glomerulopathy. However, screening is indicated for family members of affected individuals using genetic testing.


== Natural History, Complications and Prognosis==
== Natural History, Complications and Prognosis==
    
    
*Common [[Complications During and Following Cardiac Catheterization and Percutaneous Coronary Intervention|complications]] of C3 [[glomerulopathy]] include [[renal failure]], [[atherosclerosis]], and [[vision loss]]
*Common [[Complications During and Following Cardiac Catheterization and Percutaneous Coronary Intervention|complications]] of C3 [[glomerulopathy]] include [[renal failure]], [[atherosclerosis]], and [[vision loss]].<ref name="pmid22456601">{{cite journal |vauthors=Servais A, Noël LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA, Macher MA, Zuber J, Karras A, Provot F, Moulin B, Grünfeld JP, Niaudet P, Lesavre P, Frémeaux-Bacchi V |title=Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies |journal=Kidney Int. |volume=82 |issue=4 |pages=454–64 |date=August 2012 |pmid=22456601 |doi=10.1038/ki.2012.63 |url=}}</ref>
*[[Prognosis]] of [[C3 glomerulopathy]] is generally poor, and 10 ­year [[mortality]] of [[patients]] is approximately 36%.
*[[Prognosis]] of [[C3 glomerulopathy MRI|C3 glomerulopathy]] is generally poor without proper treatment.
*10 ­year [[mortality]] of [[patients]] with C3 glomerulopathy is approximately 36%.


== Diagnosis ==
== Diagnosis ==
===Diagnostic test of choice===
====Diagnostic test of choice====
Gold standard [[test]] of choice for [[C3 glomerulopathy]] is [[kidney]] [[biopsy]].
Kidney biopsy is the gold standard test for the diagnosis of [[C3 glomerulopathy MRI|C3 glomerulopathy]].


=== Symptoms ===
==== Symptoms ====
Common symptoms of [[C3 glomerulopathy MRI|C3 glomerulopathy]] may include:<ref name="pmid20301598">{{cite journal |vauthors=Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, Martín B, Smith RJH |title= |journal= |volume= |issue= |pages= |date= |pmid=20301598 |doi= |url=}}</ref><ref name="pmid27878657">{{cite journal |vauthors=Ito N, Ohashi R, Nagata M |title=C3 glomerulopathy and current dilemmas |journal=Clin. Exp. Nephrol. |volume=21 |issue=4 |pages=541–551 |date=August 2017 |pmid=27878657 |pmc=5721121 |doi=10.1007/s10157-016-1358-5 |url=}}</ref>
*Foamy [[urine]] due [[proteinuria]]
*[[Hematuria]]
*Signs of [[renal]] [[Aortic insufficiency|insufficiency]] like general [[fatigue]] or [[malaise]]
*[[Hypertension]]
*Hypocomplementimia
*Acquired [[lipodystrophy]]
*[[Macular]] ([[Drusen]]) deposits in the [[retina]] of the [[eye]]


*[[Symptoms]] of [[C3 glomerulopathy]] may include the following:
{| class="wikitable"
:*Foamy [[urine]] due [[proteinuria]] ( excessive [[protein]] in [[urine]])or [[hematuria]] (blood in the urine)<ref name="pmid20301598">{{cite journal |vauthors=Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, Martín B, Smith RJH |title= |journal= |volume= |issue= |pages= |date= |pmid=20301598 |doi= |url=}}</ref>
|+
:*Signs of [[renal]] [[Aortic insufficiency|insufficiency]] like general [[fatigue]] or [[malaise]]
!Characterstics
:*[[Hypertension]] (especially in children is a red flag )<ref name="pmid27878657">{{cite journal |vauthors=Ito N, Ohashi R, Nagata M |title=C3 glomerulopathy and current dilemmas |journal=Clin. Exp. Nephrol. |volume=21 |issue=4 |pages=541–551 |date=August 2017 |pmid=27878657 |pmc=5721121 |doi=10.1007/s10157-016-1358-5 |url=}}</ref>
!DDD
:*Low [[serum]] [[C3 convertase|C3]] level
!C3GN
:*Acquired [[lipodystrophy]] (loss of subcutaneous [[fat]] in the upper half of the body) in DDD
|-
:*[[Macular]] (Drusen) deposits in the [[retina]] of the [[eye]] (also seen in DDD)
|Mean age
|14
|24
|-
|ESRD
|50% in 10 years
|10% in 2.5 years
|-
|Associated conditions
|
* Acquired [[lipodystrophy]]
* Type 1 DM
* Macular degeneration
| -
|-
|C3 convertase dysregulation
|↑↑
|↑
|-
|C5 convertase dysregulation
|↑
|↑↑
|-
|C3NF
| +++
| +
|-
|MAC
|↑
|↑↑↑
|}


=== Physical Examination ===
==== Laboratory Findings ====
*C3 [[glomerulopathy]] is diagnosed using [[immunofluorescence]] [[microscopy]] and electron [[microscopy]].
*There are no specific findings for C3 glomerulopathy on light microscopic.
*Findings on electron [[microscopy]] include<ref name="pmid25484526">{{cite journal |vauthors=Thomas S, Ranganathan D, Francis L, Madhan K, John GT |title=Current concepts in C3 glomerulopathy |journal=Indian J Nephrol |volume=24 |issue=6 |pages=339–48 |date=November 2014 |pmid=25484526 |pmc=4244712 |doi=10.4103/0971-4065.134089 |url=}}</ref><ref name="pmid1095806">{{cite journal |vauthors=Habib R, Gubler MC, Loirat C, Mäiz HB, Levy M |title=Dense deposit disease: a variant of membranoproliferative glomerulonephritis |journal=Kidney Int. |volume=7 |issue=4 |pages=204–15 |date=April 1975 |pmid=1095806 |doi= |url=}}</ref>
**Sub-epithelial lumps
**Abnormal electron-dense material within the GBM
***Dense and linear in DDD
***Isolated in C3GN
* Findings on immunofluorescence [[microscopy]] include:
** C3 deposits along the [[Bowman's]] capsule of glomerular and tubular basement membranes.


===Appearance of the Patient===
==== Other Diagnostic tests ====
*[[Patients]] with C3 glomerulopathy usually appear cachectic.
Other diagnostic tests that can help in diagnosing C3 glomerulopathy include:
*Measurement of complement C3, [[C3 Nef]], serum factor H, CFHR ( Complement factor H-related protein)
*Serum protein electrophoresis, immunofixation and serum free light chains
*sMAC level activity
==== Physical Examination ====
Common physical examination findings of patients with C3 glomerulopathy include:


===Vital Signs===
*High [[blood pressure]]
* New onset [[hypertension]]
*[[Pallor]] skin
*[[Edema]] of extremities
*Periorbital [[Edema]]
*[[Lipodystrophy]]


===Skin===
====Imaging Findings====
* [[Pallor]]


===HEENT===
* There are no specific [[imaging]] findings associated with [[C3 glomerulopathy MRI|C3 glomerulopathy]].
* HEENT [[examination]] of [[patients]] with C3 glomerulopathy is usually normal.


===Neck===
*  
* Neck [[examination]] of [[patients]] with C3 glomerulopathy is usually normal.


===Lungs===
== Treatment ==
* Rales may be heard
 
===Heart===
* [[Cardiovascular]] [[examination]] of patients with  C3 glomerulopathy is usually normal.
 
===Abdomen===
* Edema
 
=== Laboratory Findings ===
*The following [[blood]] [[tests]] need to be done in the [[evaluation]] of [[C3 glomerulopathy]].
 
*[[CBC]]
*[[Blood glucose]] levels and Hemoglobin A1C
* [[BUN]] and [[Creatinine]] levels
* Blood levels of [[Complement]] C3, [[C3 Nef]], Serum factor H, [[CFHR]] ( Complement factor H-related protein)
* 24-hr urine protein analysis


===Imaging Findings===
===Medical Therapy===
* The mainstay of treatment for C3 glomerulopathy is pharmacotherapy.<ref name="pmid22673887">{{cite journal |vauthors=Sethi S, Fervenza FC, Zhang Y, Zand L, Vrana JA, Nasr SH, Theis JD, Dogan A, Smith RJ |title=C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up |journal=Kidney Int. |volume=82 |issue=4 |pages=465–73 |date=August 2012 |pmid=22673887 |pmc=4438675 |doi=10.1038/ki.2012.212 |url=}}</ref><ref name="pmid170185612">{{cite journal |vauthors=Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B, Grünfeld JP, Lesavre P, Noël LH, Fakhouri F |title=Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome |journal=J. Med. Genet. |volume=44 |issue=3 |pages=193–9 |date=March 2007 |pmid=17018561 |pmc=2598029 |doi=10.1136/jmg.2006.045328 |url=}}</ref>
* Pharmacotherpay can be catagorized into:
** Supportive therapy
** Specific therapy based on disease severity 


* There are no imaging findings specific to C3 glomerulopathy
==== Supportive Therapy ====
Supportive therapy include antihypertensive medications and lipid lowering
* Indicated in C3 glomerulopathy patients associated with [[Hypertension|HTN]] and [[proteinuria]].
* Preferred regimen (1): ACE-inhibitors
* Preferred regimen (2): Angiotensin-11 receptor blockers


=== Other Diagnostic Studies ===
==== Specific therapy based on disease severity  ====
*C3 glomerulopathy may also be diagnosed using light microscopy, immunofluorescence microscopy and electron microscopy
* '''Mild disease'''
*Findings on electron microscopy include mesangial proliferative glomerulonephritis, membranoproliferative glomerulonephritis and crescentic glomerulonephritis<ref name="pmid25484526">{{cite journal |vauthors=Thomas S, Ranganathan D, Francis L, Madhan K, John GT |title=Current concepts in C3 glomerulopathy |journal=Indian J Nephrol |volume=24 |issue=6 |pages=339–48 |date=November 2014 |pmid=25484526 |pmc=4244712 |doi=10.4103/0971-4065.134089 |url=}}</ref>
** Supportive therapy
* Immunofluorescence microscopy: C3 deposits along the Bowman's capsule, glomerular and tubular basement membranes
** Regular follow up
* Electron microscopy findings in Dense Deposit Disease: Electron dense material in the glomerular basement membrane, lamina densa widening. Electron dense material is absent in C3 glomerulopathy. Subepithelial "humps" are found in both C3GN and Dense deposit disease. <ref name="pmid1095806">{{cite journal |vauthors=Habib R, Gubler MC, Loirat C, Mäiz HB, Levy M |title=Dense deposit disease: a variant of membranoproliferative glomerulonephritis |journal=Kidney Int. |volume=7 |issue=4 |pages=204–15 |date=April 1975 |pmid=1095806 |doi= |url=}}</ref>
* '''Moderate disease'''
** '''Disease due to auto-antibody'''
*** Preferred regimen (1): Plasma exchange
*** Alternative regimen (1): [[Rituximab]]
*** Alternative regimen (2): [[Eculizumab]] 900 mg IV/week for 4-5 weeks followed by 1200 mg every 2 weeks for approximately one year.
** '''Disease due to factor H deficiency'''
*** Preferred regimen (1): [[Fresh frozen plasma]] 10-15 mL/ kg body weight infused regularly x 14 days
** '''Disease due to C3 mutation'''
*** Preferred regimen (1): Plasma exchange<ref name="pmid4022205">{{cite journal |vauthors=McGinley E, Watkins R, McLay A, Boulton-Jones JM |title=Plasma exchange in the treatment of mesangiocapillary glomerulonephritis |journal=Nephron |volume=40 |issue=4 |pages=385–90 |date=1985 |pmid=4022205 |doi=10.1159/000183504 |url=}}</ref><ref name="pmid12378549">{{cite journal |vauthors=Kurtz KA, Schlueter AJ |title=Management of membranoproliferative glomerulonephritis type II with plasmapheresis |journal=J Clin Apher |volume=17 |issue=3 |pages=135–7 |date=2002 |pmid=12378549 |doi=10.1002/jca.10026 |url=}}</ref><ref name="pmid21269585">{{cite journal |vauthors=Krmar RT, Holtbäck U, Linné T, Berg UB, Celsi G, Söderberg MP, Wernerson A, Szakos A, Larsson S, Skattum L, Bárány P |title=Acute renal failure in dense deposit disease: complete recovery after combination therapy with immunosuppressant and plasma exchange |journal=Clin. Nephrol. |volume=75 Suppl 1 |issue= |pages=4–10 |date=February 2011 |pmid=21269585 |doi= |url=}}</ref>
* Severe disease with rapidly progressive worsening [[renal]] function:
** Preferred regimen (1): [[Cyclophosphamide]]
** Preferred regimen (2): [[Mycophenolate sodium|Mycophenolate mofetil]]<ref name="pmid26221755">{{cite journal |vauthors=Rabasco C, Cavero T, Román E, Rojas-Rivera J, Olea T, Espinosa M, Cabello V, Fernández-Juarez G, González F, Ávila A, Baltar JM, Díaz M, Alegre R, Elías S, Antón M, Frutos MA, Pobes A, Blasco M, Martín F, Bernis C, Macías M, Barroso S, de Lorenzo A, Ariceta G, López-Mendoza M, Rivas B, López-Revuelta K, Campistol JM, Mendizábal S, de Córdoba SR, Praga M |title=Effectiveness of mycophenolate mofetil in C3 glomerulonephritis |journal=Kidney Int. |volume=88 |issue=5 |pages=1153–60 |date=November 2015 |pmid=26221755 |doi=10.1038/ki.2015.227 |url=}}</ref>


== Treatment ==
=== Surgery ===
=== Medical Therapy ===
* Surgical intervention is not recommended for the management of C3 glomerulopathy
*Treatment is based on type of C3 glomerulopathy, severity and available treatment modalities.
*Adequate control of proteinuria and hypertension is important. T.
*Patients with DDD or C3GN may be treated with lipid lowering medications to prevent cardiovascular events.
*All patients should be closely monitored with scheduled checkups and diagnostic laboratory workups.
*Genetic screening is also advised for family members of patients that have genetic mutations.
*Patients’ support groups can be found with groups like NEPHCURE Kidney International and other foundation that provide support for kidney patients and their families.


=== Prevention ===
=== Prevention ===
*There are no primary preventive measures available for C3 glomerulopathy .
*There are no [[primary]] [[preventive]] measures available for [[C3 glomerulopathy MRI|C3 glomerulopathy]].
*Effective measures for the primary prevention of [disease name] include [measure1], [measure2], and [measure3].
 
*Once diagnosed and successfully treated, patients with [disease name] are followed-up every [duration]. Follow-up testing includes [test 1], [test 2], and [test 3].


==References==
==References==

Latest revision as of 00:39, 3 August 2020

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Vindhya BellamKonda, M.B.B.S [2] Aditya Ganti M.B.B.S. [3]

For more information of Complement mediated glomerular disorders, Click here

Synonyms and keywords: Glomerulonephritis; C3 glomerulonephritis; dense deposit disease

Overview

C3 glomerulopathy is a complement system dysregulatory disorder resulting in abnormal activation of the alternative pathway. C3 glomerulopathy includes C3 glomerulonephritis (C3GN) and dense deposit disease (DDD). Both, C3GN and dense deposit disease are characterized by marked by C3 deposition along the capillary loop, the basement membrane, and the mesangium. Identification of C3 deposits without any concomitant immunoglobulin deposition is characteristic for diagnosing C3 glomerulopathy. The activation of the alternative pathway of the complement system can be either due to inherited, or acquired defects of the complement system. Gene mutations are the most common inherited causes while autoimmune disorders are responsible for acquired glomerulopathy.

Historical Perspective

Classification

  • Initially, C3 glomerulopathy was categorized as a variant of MPGN, namely MPGN type 2. [5][6]
  • However in 2007, Servais A. et al described C3GN as an separate entity.
  • C3 Glomerulopathy may be classified into 2 main subtypes based on the appearance of complement deposition in the glomerular basement membrane on EM:
    • Dense deposit disease (DDD)
      • Dense deposition of compliment in linear pattern.
    • C3 Glomerulonephritis (C3GN)
      • Isolated deposition of C3.

Pathophysiology

  • Excessive activation of the alternative complement pathway is the inciting event in the pathogenesis of C3 glomerulopathy.[7]
  • Activation of alternative pathway results in excessive deposition of complement along the glomerular basement membrane.
  • Pattern of compliment deposition is regulated by:[8]
    • Leukocytic chemotaxis
    • Cytolytic effects of C5b-9

Physiology

Pathogenesis

  • Any mechanism by which C3 activity is increased leads to activation of alternate pathway activation resulting in complement deposition.[10][11]
    • C3 convertase autoantibody C3 nephritic factor
    • Loss of factor H

Causes

Common causes of C3 glomerulopathy include:[12]

  • C3 mutations
  • Mutation of Factor H (CHF)[13]
    • CFH is a small glycoprotein which is produced in the liver, and circulates freely in the blood plasma .
    • Primary role of factor H is to inhibit C3 convertase and thus not activating alternative complement pathway.
    • Two types of mutations are of important significance
      • Type 1 mutations are associated with decreased levels of CFH.
      • Type 2 mutations decrease or diminish the functional activity of CHF.
    • Autoantibodies against CFH. [14]
  • Auto antibody against C3 called as nephritic factor (C3bBb antibody).[15]

Differentiating C3 Glomerulopathy from other Diseases
Medical condition Differentiating features
C3 glomerulopathy
  • Persistent glomerulonephritis over prolonged period
  • Decreased C3 levels persist
  • Immunofluorescence microscopy shows intense C3 staining without immunoglobulin staining.
Lupus nephritis
  • Anti C1q autoantibodies
  • Immune complex glomerulonephritis
  • Glomerular deposits of IgG, IgM, IgA, C3 and C1q
Poststreptococcal glomerulonephritis
  • Glomeruonephritis in most cases resolves after infection subsides
  • Decreased levels of C3 is transient
  • Immunoflouroescence microscopy shows immunoglobulin deposition in poststreptococcal infection
Staphylococcal associated glomerulonephritis
  • Glomerulonephritis resolves after infection subsides
  • Decreased C3 is transient
  • Immunofluorescence microscopy shows immunoglobulin deposition in staphylococcal associated glomerulonephritis.

Epidemiology and Demographics

Risk Factors

Common risk factors in the development of C3 glomerulopathy include:

Screening

  • There is insufficient evidence to recommend routine screening for C3 glomerulopathy. However, screening is indicated for family members of affected individuals using genetic testing.

Natural History, Complications and Prognosis

Diagnosis

Diagnostic test of choice

Kidney biopsy is the gold standard test for the diagnosis of C3 glomerulopathy.

Symptoms

Common symptoms of C3 glomerulopathy may include:[18][19]

Characterstics DDD C3GN
Mean age 14 24
ESRD 50% in 10 years 10% in 2.5 years
Associated conditions -
C3 convertase dysregulation ↑↑ ↑
C5 convertase dysregulation ↑ ↑↑
C3NF +++ +
MAC ↑ ↑↑↑

Laboratory Findings

  • C3 glomerulopathy is diagnosed using immunofluorescence microscopy and electron microscopy.
  • There are no specific findings for C3 glomerulopathy on light microscopic.
  • Findings on electron microscopy include[20][21]
    • Sub-epithelial lumps
    • Abnormal electron-dense material within the GBM
      • Dense and linear in DDD
      • Isolated in C3GN
  • Findings on immunofluorescence microscopy include:
    • C3 deposits along the Bowman's capsule of glomerular and tubular basement membranes.

Other Diagnostic tests

Other diagnostic tests that can help in diagnosing C3 glomerulopathy include:

  • Measurement of complement C3, C3 Nef, serum factor H, CFHR ( Complement factor H-related protein)
  • Serum protein electrophoresis, immunofixation and serum free light chains
  • sMAC level activity

Physical Examination

Common physical examination findings of patients with C3 glomerulopathy include:

Imaging Findings

Treatment

Medical Therapy

  • The mainstay of treatment for C3 glomerulopathy is pharmacotherapy.[22][23]
  • Pharmacotherpay can be catagorized into:
    • Supportive therapy
    • Specific therapy based on disease severity

Supportive Therapy

Supportive therapy include antihypertensive medications and lipid lowering

  • Indicated in C3 glomerulopathy patients associated with HTN and proteinuria.
  • Preferred regimen (1): ACE-inhibitors
  • Preferred regimen (2): Angiotensin-11 receptor blockers

Specific therapy based on disease severity

  • Mild disease
    • Supportive therapy
    • Regular follow up
  • Moderate disease
    • Disease due to auto-antibody
      • Preferred regimen (1): Plasma exchange
      • Alternative regimen (1): Rituximab
      • Alternative regimen (2): Eculizumab 900 mg IV/week for 4-5 weeks followed by 1200 mg every 2 weeks for approximately one year.
    • Disease due to factor H deficiency
      • Preferred regimen (1): Fresh frozen plasma 10-15 mL/ kg body weight infused regularly x 14 days
    • Disease due to C3 mutation
  • Severe disease with rapidly progressive worsening renal function:

Surgery

  • Surgical intervention is not recommended for the management of C3 glomerulopathy

Prevention

References

  1. ↑ SELIGMANN M, HANAU C (1958). "[Immuno-electrophoretic study of the blood of disseminated lupus erythematosus patients]". Rev Hematol (in French). 13 (2): 239–48. PMID 13568372.
  2. ↑ WEST CD, NORTHWAY JD, DAVIS NC (August 1964). "SERUM LEVELS OF BETA-1C GLOBULIN, A COMPLEMENT COMPONENT, IN THE NEPHRITIDES, LIPOID NEPHROSIS, AND OTHER CONDITIONS". J. Clin. Invest. 43: 1507–17. doi:10.1172/JCI105027. PMC 441951. PMID 14201535.
  3. ↑ BERGER J, GALLE P (1962). "[Unusual change of the basal membranes of the kidney]". J Urol Nephrol (Paris). 68: 116–22. PMID 13867660.
  4. ↑ Fakhouri F, Frémeaux-Bacchi V, Noël LH, Cook HT, Pickering MC (August 2010). "C3 glomerulopathy: a new classification". Nat Rev Nephrol. 6 (8): 494–9. doi:10.1038/nrneph.2010.85. PMID 20606628.
  5. ↑ Appel GB, Cook HT, Hageman G, Jennette JC, Kashgarian M, Kirschfink M, Lambris JD, Lanning L, Lutz HU, Meri S, Rose NR, Salant DJ, Sethi S, Smith RJ, Smoyer W, Tully HF, Tully SP, Walker P, Welsh M, Würzner R, Zipfel PF (May 2005). "Membranoproliferative glomerulonephritis type II (dense deposit disease): an update". J. Am. Soc. Nephrol. 16 (5): 1392–403. doi:10.1681/ASN.2005010078. PMID 15800116.
  6. ↑ Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B; et al. (2007). "Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome". J Med Genet. 44 (3): 193–9. doi:10.1136/jmg.2006.045328. PMC 2598029. PMID 17018561.
  7. ↑ Schwertz R, de Jong R, Gretz N, Kirschfink M, Anders D, Schärer K (March 1996). "Outcome of idiopathic membranoproliferative glomerulonephritis in children. Arbeitsgemeinschaft Pädiatrische Nephrologie". Acta Paediatr. 85 (3): 308–12. PMID 8695987.
  8. ↑ Thomas S, Ranganathan D, Francis L, Madhan K, John GT (November 2014). "Current concepts in C3 glomerulopathy". Indian J Nephrol. 24 (6): 339–48. doi:10.4103/0971-4065.134089. PMC 4244712. PMID 25484526.
  9. ↑ Noris M, Remuzzi G (November 2013). "Overview of complement activation and regulation". Semin. Nephrol. 33 (6): 479–92. doi:10.1016/j.semnephrol.2013.08.001. PMC 3820029. PMID 24161035.
  10. ↑ Thomas S, Ranganathan D, Francis L, Madhan K, John GT (November 2014). "Current concepts in C3 glomerulopathy". Indian J Nephrol. 24 (6): 339–48. doi:10.4103/0971-4065.134089. PMC 4244712. PMID 25484526.
  11. ↑ Bomback AS, Appel GB (November 2012). "Pathogenesis of the C3 glomerulopathies and reclassification of MPGN". Nat Rev Nephrol. 8 (11): 634–42. doi:10.1038/nrneph.2012.213. PMID 23026947.
  12. ↑ Holers VM (June 2013). "Human C3 glomerulopathy provides unique insights into complement factor H-related protein function". J. Clin. Invest. 123 (6): 2357–60. doi:10.1172/JCI69684. PMC 3668810. PMID 23728171.
  13. ↑ Rodríguez de Córdoba S, Esparza-Gordillo J, Goicoechea de Jorge E, Lopez-Trascasa M, Sánchez-Corral P (June 2004). "The human complement factor H: functional roles, genetic variations and disease associations". Mol. Immunol. 41 (4): 355–67. doi:10.1016/j.molimm.2004.02.005. PMID 15163532.
  14. ↑ Noris M, Donadelli R, Remuzzi G (June 2018). "Autoimmune abnormalities of the alternative complement pathway in membranoproliferative glomerulonephritis and C3 glomerulopathy". Pediatr. Nephrol. doi:10.1007/s00467-018-3989-0. PMID 29948306.
  15. ↑ Togarsimalemath SK, Sethi SK, Duggal R, Le Quintrec M, Jha P, Daniel R, Gonnet F, Bansal S, Roumenina LT, Fremeaux-Bacchi V, Kher V, Dragon-Durey MA (October 2017). "A novel CFHR1-CFHR5 hybrid leads to a familial dominant C3 glomerulopathy". Kidney Int. 92 (4): 876–887. doi:10.1016/j.kint.2017.04.025. PMID 28729035.
  16. ↑ Smith RJ, Alexander J, Barlow PN, Botto M, Cassavant TL, Cook HT; et al. (2007). "New approaches to the treatment of dense deposit disease". J Am Soc Nephrol. 18 (9): 2447–56. doi:10.1681/ASN.2007030356. PMC 4853920. PMID 17675665.
  17. ↑ Servais A, Noël LH, Roumenina LT, Le Quintrec M, Ngo S, Dragon-Durey MA, Macher MA, Zuber J, Karras A, Provot F, Moulin B, Grünfeld JP, Niaudet P, Lesavre P, Frémeaux-Bacchi V (August 2012). "Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies". Kidney Int. 82 (4): 454–64. doi:10.1038/ki.2012.63. PMID 22456601.
  18. ↑ Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean L, Stephens K, Amemiya A, Martín B, Smith R. PMID 20301598. Vancouver style error: initials (help); Missing or empty |title= (help)
  19. ↑ Ito N, Ohashi R, Nagata M (August 2017). "C3 glomerulopathy and current dilemmas". Clin. Exp. Nephrol. 21 (4): 541–551. doi:10.1007/s10157-016-1358-5. PMC 5721121. PMID 27878657.
  20. ↑ Thomas S, Ranganathan D, Francis L, Madhan K, John GT (November 2014). "Current concepts in C3 glomerulopathy". Indian J Nephrol. 24 (6): 339–48. doi:10.4103/0971-4065.134089. PMC 4244712. PMID 25484526.
  21. ↑ Habib R, Gubler MC, Loirat C, Mäiz HB, Levy M (April 1975). "Dense deposit disease: a variant of membranoproliferative glomerulonephritis". Kidney Int. 7 (4): 204–15. PMID 1095806.
  22. ↑ Sethi S, Fervenza FC, Zhang Y, Zand L, Vrana JA, Nasr SH, Theis JD, Dogan A, Smith RJ (August 2012). "C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-up". Kidney Int. 82 (4): 465–73. doi:10.1038/ki.2012.212. PMC 4438675. PMID 22673887.
  23. ↑ Servais A, Frémeaux-Bacchi V, Lequintrec M, Salomon R, Blouin J, Knebelmann B, Grünfeld JP, Lesavre P, Noël LH, Fakhouri F (March 2007). "Primary glomerulonephritis with isolated C3 deposits: a new entity which shares common genetic risk factors with haemolytic uraemic syndrome". J. Med. Genet. 44 (3): 193–9. doi:10.1136/jmg.2006.045328. PMC 2598029. PMID 17018561.
  24. ↑ McGinley E, Watkins R, McLay A, Boulton-Jones JM (1985). "Plasma exchange in the treatment of mesangiocapillary glomerulonephritis". Nephron. 40 (4): 385–90. doi:10.1159/000183504. PMID 4022205.
  25. ↑ Kurtz KA, Schlueter AJ (2002). "Management of membranoproliferative glomerulonephritis type II with plasmapheresis". J Clin Apher. 17 (3): 135–7. doi:10.1002/jca.10026. PMID 12378549.
  26. ↑ Krmar RT, Holtbäck U, Linné T, Berg UB, Celsi G, Söderberg MP, Wernerson A, Szakos A, Larsson S, Skattum L, Bárány P (February 2011). "Acute renal failure in dense deposit disease: complete recovery after combination therapy with immunosuppressant and plasma exchange". Clin. Nephrol. 75 Suppl 1: 4–10. PMID 21269585.
  27. ↑ Rabasco C, Cavero T, Román E, Rojas-Rivera J, Olea T, Espinosa M, Cabello V, Fernández-Juarez G, González F, Ávila A, Baltar JM, Díaz M, Alegre R, Elías S, Antón M, Frutos MA, Pobes A, Blasco M, Martín F, Bernis C, Macías M, Barroso S, de Lorenzo A, Ariceta G, López-Mendoza M, Rivas B, López-Revuelta K, Campistol JM, Mendizábal S, de Córdoba SR, Praga M (November 2015). "Effectiveness of mycophenolate mofetil in C3 glomerulonephritis". Kidney Int. 88 (5): 1153–60. doi:10.1038/ki.2015.227. PMID 26221755.
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